GLPBio

Anhydrosafflor yellow B

Catalog No.: GC60587Purity:>98.00%Synonyms: AHSYB
Anhydrosafflor yellow B (AHSYB) es un glucÓsido C de quinocalcona aislado de Carthamus tinctorius.

Los productos son exclusivamente para uso en investigación. No aptos para uso humano. No vendemos a pacientes.


Anhydrosafflor yellow B
Cas No.: 184840-84-4
1mgIn Stock
$108.00
1
5mgIn Stock
$270.00
1

Citas (Citations)

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    Nature
    641, 529–536 (2025)
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    628, 630–638 (2024)
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    632, 686–694 (2024)
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    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    388(6745) (2025)
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    387(6734) (2025)
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    35, 97–116 (2025)
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    34, 683–706 (2024)
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    Cell Research
    31, 1291–1307 (2021)

Descripción (Description)

Anhydrosafflor yellow B is a quinolone C-glycoside isolated from safflower (Carthamus tinctorius). Anhydrosafflor yellow B inhibits ADP-induced platelet aggregation and possesses antioxidant and neuroprotective effects. Anhydrosafflor yellow B can be used in neuroscience and neurological disease research[1-4].

In vitro, Anhydrosafflor yellow B (100–200μM) pretreated a neuron-astrocyte co-culture system for 2 hours, followed by stimulation with 6-OHDA (10μM) for 24 hours. Anhydrosafflor yellow B significantly reduced neuronal apoptosis rate, increased cell survival rate, and decreased IL-1β and IL-10 levels[5]. Anhydrosafflor yellow B (50–200μM) pretreated differentiated PC12 cells for 6 hours, followed by stimulation with Rotenone (0.5μM) for 24 hours. Anhydrosafflor yellow B significantly increased cell viability and suppressed the decreased cell area induced by Rotenone[6].

In vivo, Anhydrosafflor yellow B (50μmol/kg; single injection) was intraperitoneally administered to C57BL/6J mice with acute lung injury model. Anhydrosafflor yellow B alleviated lung histopathological changes in mice, inhibited the production of tumor necrosis factor-α and interleukin-6, reduced the lung wet-to-dry weight ratio and protein concentration in bronchoalveolar lavage fluid, decreased the number of total cells and neutrophils in bronchoalveolar lavage fluid, and suppressed the co-localization of myeloperoxidase and histone as well as the formation of myeloperoxidase-DNA complexes[7]. Anhydrosafflor yellow B (2, 4, 8mg/kg; once daily) was intravenously injected via the tail vein to Sprague-Dawley rats with middle cerebral artery occlusion/reperfusion model for 4 consecutive days. Anhydrosafflor yellow B effectively reduced infarct volume, improved neurological function, inhibited apoptosis, and decreased oxidative stress response[8].

References:
[1] Chen G, Li C, Zhang L, et al. Hydroxysafflor yellow A and anhydrosafflor yellow B alleviate ferroptosis and parthanatos in PC12 cells injured by OGD/R. Free Radic Biol Med. 2022 Feb 1;179:1-10.
[2] Ablat N, Liu R, Ablimit M, et al. Preventive effects of a standardized flavonoid extract of safflower in rotenone-induced Parkinson's disease rat model. Neuropharmacology. 2022 Oct 1;217:109209.
[3] Zhou J, Zhou C, Chen Q, et al. Integrating in silico and experimental approaches to uncover the anti-apoptotic effects of anhydrosafflor yellow B via JNK/Bid pathway in ischemic stroke. Brain Res. 2025 Nov 15;1867:149947.
[4] Yue S, Wu L, Wang J, et al. Metabolic profile of anhydrosafflor yellow B in rats by ultra-fast liquid chromatography/quadrupole time-of-flight mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci. 2016 Mar 1;1014:37-44.
[5] Lei H, Ren R, Sun Y, et al. Neuroprotective Effects of Safflower Flavonoid Extract in 6-Hydroxydopamine-Induced Model of Parkinson's Disease May Be Related to its Anti-Inflammatory Action. Molecules. 2020 Nov 9;25(21):5206.
[6] Ren R, Shi C, Cao J, et al. Neuroprotective Effects of A Standardized Flavonoid Extract of Safflower Against Neurotoxin-Induced Cellular and Animal Models of Parkinson's Disease. Sci Rep. 2016 Feb 24;6:22135.
[7] Wang YP, Guo Y, Wen PS, et al. Three Ingredients of Safflower Alleviate Acute Lung Injury and Inhibit NET Release Induced by Lipopolysaccharide. Mediators Inflamm. 2020 Feb 29;2020:2720369.
[8] Fangma Y, Zhou H, Shao C, et al. Hydroxysafflor Yellow A and Anhydrosafflor Yellow B Protect Against Cerebral Ischemia/Reperfusion Injury by Attenuating Oxidative Stress and Apoptosis via the Silent Information Regulator 1 Signaling Pathway. Front Pharmacol. 2021 Sep 30;12:739864.

Protocolo (Protocol)

Cell experiment [1]:

Cell lines

Differentiated PC12 cells

Preparation Method

Differentiated PC12 cells were pretreated with Anhydrosafflor yellow B at concentrations ranging from 50 to 200μM for 6 hours and subsequently treated with 0.5μM Rotenone for 24 hours.

Reaction Conditions

50-200μM; pretreatment for 6 hours

Applications

Anhydrosafflor yellow B at 200μM concentration significantly increased cell viability. Anhydrosafflor yellow B significantly suppressed the decreased cell area induced by rotenone.

Animal experiment [2]:

Animal models

C57BL/6J mice

Preparation Method

Mice were anesthetized and received intratracheal injection of LPS (10mg/kg) to induce acute lung injury. Anhydrosafflor yellow B was administered intraperitoneally immediately after LPS injection.

Dosage form

50μmol/kg; i.p.; single administered immediately after LPS injection

Applications

Anhydrosafflor yellow B alleviated LPS-induced lung histopathologic changes, suppressed inflammatory cytokine (TNF-α and IL-6) production in plasma and bronchoalveolar lavage fluid, protected lung permeability (reduced wet-to-dry weight ratio and total protein concentration in bronchoalveolar lavage fluid), blocked inflammatory cell infiltration (reduced total cells and neutrophils in bronchoalveolar lavage fluid), inhibited neutrophil extracellular trap formation in lungs, decreased neutrophil extracellular trap levels in plasma, and suppressed the Raf/MEK/ERK signaling pathway in lung tissue.

References:
[1] Ren R, Shi C, Cao J, et al. Neuroprotective Effects of A Standardized Flavonoid Extract of Safflower Against Neurotoxin-Induced Cellular and Animal Models of Parkinson's Disease. Sci Rep. 2016 Feb 24;6:22135.
[2] Wang YP, Guo Y, Wen PS, et al. Three Ingredients of Safflower Alleviate Acute Lung Injury and Inhibit NET Release Induced by Lipopolysaccharide. Mediators Inflamm. 2020 Feb 29;2020:2720369.

Documentos del producto (Product Documents)

Purity:>98.00%Appearance:A solid

Propiedades químicas (Chemical Properties)

N.º CAS
184840-84-4
Sinónimos
AHSYB
SMILES
OC[C@@H](O)[C@@H](O)[C@@H]([C@]1([H])[C@](C2=C(C(C(O)=C(C2=O)C(/C=C/C3=CC=C(C=C3)O)=O)([C@]4([H])O[C@@H]([C@H]([C@@H]([C@H]4O)O)O)CO)O)O)([H])C5=C(C(C(O)=C(C5=O)C(/C=C/C6=CC=C(C=C6)O)=O)([C@]7([H])O[C@@H]([C@H]([C@@H]([C@H]7O)O)O)CO)O)O1)O
Fórmula molecular
C48H52O26
Peso molecular
1044.91
Almacenamiento
Store at -20°C
Consejos generales
Seleccione un disolvente adecuado según los datos de solubilidad del producto. Una vez preparada, divida la solución madre en alícuotas para evitar ciclos repetidos de congelación y descongelación.
Utilice las soluciones madre en un plazo de 6 meses si se conservan a -80°C, o de 1 mes si se conservan a -20°C.
Para mejorar la solubilidad, caliente el tubo a 37°C y soníquelo durante un periodo adecuado.
Condiciones de envío
Las muestras de evaluación se envían con acumuladores de frío. Los demás tamaños se envían a temperatura ambiente o, previa solicitud, con acumuladores de frío.

Calculadoras (Calculators)Molaridad / Dilución / Peso molecular / Conversión de unidades / Formulación in vivo / Solubilidad

g/mol

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